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The Top 10 Things You Need To Know About The OIG's Revised Self-Disclosure Protocol
1. PattonBoggs.com Health Care, FDA and Life Sciences Client Alert 1
APRIL 18, 2013
This Alert provides only general
information and should not be
relied upon as legal advice. This
Alert may be considered attorney
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authors listed below.
LAURENCE FREEDMAN
lfreedman@pattonboggs.com
LAURA LAEMMLE -
WEIDENFELD
lweidenfeld@pattonboggs.com
CAITLIN MCCORMICK
cmccormick@pattonboggs.com
ABU DHABI
ANCHORAGE
DALLAS
DENVER
DOHA
DUBAI
NEW JERSEY
NEW YORK
RIYADH
WASHINGTON DC
HEALTH CARE, FDA AND LIFE SCIENCES CLIENT ALERT
THE TOP 10 THINGS YOU NEED TO
KNOW ABOUT THE OIG’S REVISED
SELF-DISCLOSURE PROTOCOL
On Wednesday, April 17, 2013, the Department of Health and Human Services’
Office of Inspector General (OIG) released an updated Self-Disclosure Protocol
(SDP) governing the process by which health care providers can voluntarily
identify, disclose, and resolve situations involving potential fraud involving a
Federal health care program (FHCP), such as Medicare and Medicaid. This release
builds on the initial SDP created in 1998, as well as additional guidance from OIG
published in a series of open letters in 2006, 2008 and 2009. The OIG decided to
revise the SDP in its entirety, and the revised SDP supersedes and replaces the
prior SDP and open letters.
As a practical matter, the newly released SDP does not fundamentally change the
system for provider self-disclosures. The OIG reaffirms that all health care
providers, suppliers, or other individuals or entities who are subject to OIG’s
CMP authorities, found at 42 C.F.R. Part 1003, are eligible to use the SDP. The
OIG also reaffirms that the SDP is available to facilitate the resolution of matters
that, in the disclosing party’s reasonable assessment, “potentially violate Federal
criminal, civil, or administrative laws for which CMPs are authorized.”
There are, however, several important new elements included in the SDP that will
impact providers who are considering using the SDP. These new, key changes to
the SDP include the following:
1. Minimum Multiplier of 1.5: For the first time, OIG specifies that its
“general practice is to require a minimum multiplier of 1.5 times the singles
damages” in any given matter, which is lower than what would “normally” be
required in a government-initiated investigation. OIG also specifies that generally
it applies the 1.5 multiplier to the amount paid by FHCPs and not to the amount
claimed by the provider. The OIG states that the specific multiplier it uses will
2. PattonBoggs.com Health Care, FDA and Life Sciences Client Alert 2
vary depending on the facts of each situation, and higher multipliers may be warranted in some
circumstances.
2. Requires Acknowledgement of Potential Violation: The OIG states that it will not accept any disclosing
party into the SDP if the disclosure involves the Anti-Kickback Statute (AKS) (42 USC §1320a-7b) and/or
the Stark Law (42 USC §1395nn) and the discloser fails to acknowledge clearly that the disclosed arrangement
“constitutes a potential violation of the AKS and, if applicable, the Stark Law.
3. Internal Investigations Must be Certified as Complete within 90 Days of Submission: OIG has always
required providers utilizing the SDP to conduct an internal investigation and report findings as part of the
SDP process. OIG now specifies that if a provider has not completed its investigation before it submits to
the SDP, then the provider must certify that it will complete the investigation within 90 days of initial
submission. The OIG does not explicitly state that extensions will be granted if appropriate under the
circumstances, or what it expects to happen if an investigation is conducted diligently but cannot be
completed in 90 days due to the complexity of the matter or other reasonable circumstances.
4. Providers Must Address Specific Factors in the Kickback Analysis: While OIG has always required
providers to include a description of the conduct that is the subject of the disclosure, the new SDP
emphasizes that providers must describe the “precise nature of the disclosed conduct” including a “concise
statement of all details directly relevant to the disclosed conduct” and a “specific analysis” of why the
disclosed conduct potentially violates the AKS and the Stark Law .
OIG also lists the following as examples of the types of information it may find useful in assessing and
resolving disclosed conduct involving the AKS and, if applicable, the Stark Law: (1) how fair market value
was determined, and why it is now in question; (2) why required payments from referral sources, under leases
or other contracts, were not timely made or collected, or did not conform to the negotiated agreement, and
for how long such lapses existed; (3) why the arrangement was arguably not commercially reasonable (e.g. it
lacked a reasonable business purpose); (4) whether payments were made for services not performed or
documented, and, if so, why; (5) whether referring physicians received payments from Designated Health
Service entities that varied with, or took into account, the volume or value of referrals without complying
with a Stark Law exception; and (6) the corrective action taken and any safeguards implemented to prevent a
reoccurrence.
5. Process for Calculating Damages for Disclosures Involving the AKS and Stark Law: The new SDP
provides a specific process for calculating damages in submissions that involve violations of the AKS alone or
the AKS and the Stark Law. The submitter must calculate the total amount paid by FHCPs using as an
estimate, the OIG’s specified methodology, or another reliable methodology, which must then be explained
3. PattonBoggs.com Health Care, FDA and Life Sciences Client Alert 3
in the submission. Disclosing parties also must specify the total amount of remuneration involved in an
arrangement, regardless of whether a portion of that remuneration was not in violation of the AKS or Stark
Law. OIG confirms that to resolve SDP matters involving the AKS it generally compromises its CMP
authorities for an amount based on a multiplier of the remuneration conferred by the referral recipient to the
individual or entity making the referral. Submitters can argue, however, that a portion of the total
remuneration should not be considered in calculating damages. OIG reiterates that it has discretion in
determining the appropriate amount of damages that will be required to resolve the matter.
6. Specific Instructions for Disclosures Regarding Excluded Persons: In the prior SDP, OIG did not
specifically address what information would have to be disclosed in reports regarding employment of, or
contracting with, an excluded party. The SDP now includes a section detailing the requirements for such
disclosures. Providers must disclose: (1) the identity of the excluded individual and any provider ID number;
(2) the individual’s job duties; (3) the dates the individual was employed or under contract; (4) a description of
any background checks completed before and/or during the time the individual was employed or under
contract; (5) a description of the provider’s screening process and what led to the hiring or contracting with
the excluded individual; (6) a description of how the situation was discovered; and (7) a description of
corrective action taken.
The new SDP also specifies how damages should be calculated in disclosures involving employment of, or
contracting with, an excluded party. Where the items or services furnished, ordered or prescribed by the
excluded individual were separately billed to a FHCP, the disclosure should specify the total amount claimed
and paid by the FHCP. OIG notes that this approach will likely apply when the excluded party is a direct
provider, such as a physician or pharmacist. In situations where the excluded party is providing items and
services that are not separately billed to an FHCP, however, OIG acknowledges that calculating damages can
be difficult. For purposes of resolving SDP matters involving these non-separately-billable items or services,
the OIG will use the disclosing party’s total costs of employment or contracting during the exclusion to
estimate the value of the items of services provided by that excluded individual.
7. $10,000 Minimum Settlement Amount for Non-Kickback Submissions: Consistent with the 2009 Open
Letter to Health Care Providers, the new SDP specifies that, for kickback-related submissions, OIG will
require a minimum settlement of $50,000, consistent with its CMP penalty authority. The new SDP
announces for the first time, however, that, for all other matters, the minimum settlement amount will be
$10,000, also based on OIG’s CMP penalty authority
8. Tolling the Statute of Limitations: The new SDP specifies that the disclosing parties must agree to waive
and not plead statute of limitations, laches or any similar defense to any administrative action filed by the
4. PattonBoggs.com Health Care, FDA and Life Sciences Client Alert 4
OIG “relating to the disclosed conduct,” except to the extent that such defenses were available to the
disclosing party on the date of submission.
9. Advocating to DOJ for Benefits for Disclosing Parties: In the new SDP, OIG states that, in coordinating
with DOJ in both civil and criminal matters, it will “advocate” that disclosing parties should receive a benefit
from disclosing under the SDP. For civil matters, OIG will advocate for allowing the matter to be resolved
“consistent with OIG’s approach in similar cases.”
10. CIAs Not Required to Resolve SDP Matters: OIG confirms its earlier statement in a 2008 Open Letter to
Health Care Providers that it has a presumption against requiring Corporate Integrity Agreements (CIAs) as a
condition for resolving SDP matters. In 2006, prior to implementing this policy in 2008, OIG required CIAs
in 27 of the 136 self-disclosures that it resolved with a monetary payment. Since 2008, however, OIG has
required specific integrity measures in only one of the 235 SDP matters that it resolved.
The revised SDP clarifies a number of standing practices, and also makes new policy announcements. OIG states in
the SDP that it will not accept submissions involving only Stark Law violations without any AKS component to them.
Also, consistent with the February 2012 Notice of Proposed Rulemaking from the Centers for Medicare and
Medicaid, OIG confirms that the provider’s obligation to report and return identified overpayments within 60 days is
suspended if the submission to the SDP is timely made and OIG acknowledges receipt of the submission. OIG also
indicates that it is making efforts to streamline its internal process for reviewing and resolving SDPs and states that
the current average time between acceptance into the program and resolution is 12 months.
Under the revised protocol, providers considering the SDP program will have more specific details to guide their
submission, but will also face stricter requirements, such as the 90 day timeline for completing internal investigations.
Providers facing a potential disclosure should discuss whether the SDP process is available under any specific
circumstances, as well as the benefits and risks of a potential self-disclosure, with counsel before invoking the SDP
process.